Description

O-Acetyl-N-(p-nitrobenzoyl)hydroxylamine (CAS No. 1613-81-6) is a high-purity chemical reagent with the molecular formula C₉H₈N₂O₅. This compound is widely utilized in organic synthesis, pharmaceutical research, and biochemical applications due to its unique nitrobenzoyl and acetyloxy functional groups. It serves as a versatile intermediate for the development of novel compounds, particularly in the synthesis of amides, esters, and hydroxamic acid derivatives. With a molecular weight of 224.17 g/mol, this product is supplied as a crystalline solid with guaranteed >98% purity, ensuring optimal performance in sensitive reactions. Suitable for use in analytical standards, catalyst development, and medicinal chemistry, this reagent is packaged under inert conditions to maintain stability and shelf life. Store in a cool, dry place away from light and moisture for prolonged integrity.

Properties

• CAS Number: 1613-81-6
• Complexity: 291
• IUPAC Name: [(4-nitrobenzoyl)amino] acetate
• InChI: InChI=1S/C9H8N2O5/c1-6(12)16-10-9(13)7-2-4-8(5-3-7)11(14)15/h2-5H,1H3,(H,10,13)
• InChI Key: DGCQHHXNQRYLBM-UHFFFAOYSA-N
• Exact Mass: 224.04332136
• Molecular Formula: C9H8N2O5
• Molecular Weight: 224.17
• SMILES: CC(=O)ONC(=O)C1=CC=C(C=C1)[N+](=O)[O-]
• Topological: 101
• Monoisotopic Mass: 224.04332136
• Synonyms: 1613-81-6, O-Acetyl-N-(p-nitrobenzoyl)hydroxylamine, [(4-nitrobenzoyl)amino] acetate, N-Acetyloxy-p-nitrobenzamide, BRN 1986770, n-(acetyloxy)-4-nitrobenzamide, O-Acetyl-p-nitrobenzohydroxamate, Hydroxylamine, O-acetyl-N-(p-nitrobenzoyl)-, (4-NITROPHENYL)FORMAMIDO ACETATE, SCHEMBL11747923, DTXSID60936477, CCG-56085, SR-01000645068-1

O-Acetyl-N-(p-nitrobenzoyl)hydroxylamine is primarily employed as a key intermediate in the synthesis of hydroxamic acid derivatives, which are pivotal in metalloproteinase inhibition studies. It is also used in pharmaceutical research for developing protease inhibitors and anti-inflammatory agents. Additionally, this compound finds applications in material science for modifying polymer surfaces and enhancing catalytic properties. Its reactivity with nucleophiles makes it valuable for cross-coupling reactions in organic chemistry.

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